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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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Z-1654-2022 - Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. 1 09/09/2022 Philips Respironics, Inc.
Z-1655-2022 - Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. 1 09/09/2022 Philips Respironics, Inc.
Z-1659-2022 - Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. 1 09/09/2022 Philips Respironics, Inc.
Z-1657-2022 - Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. 1 09/09/2022 Philips Respironics, Inc.
Z-1658-2022 - Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. 1 09/09/2022 Philips Respironics, Inc.
Z-1656-2022 - Philips BiPAP V30 Auto, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. 1 09/09/2022 Philips Respironics, Inc.
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